PubMed (GeneRIF) for id: 1184

Year	Number of Results
2003	7
2004	5
2005	3
2006	4
2007	5
2008	3
2009	9
2010	7
2011	2
2012	3
2013	4
2014	5
2015	1
2016	2
2017	5
2018	2
2019	3
2020	6
2023	3
2024	0

1

Human parietal epithelial cells (PECs) and proteinuria in lupus nephritis: a role for ClC-5, megalin, and cubilin?

Ceol M, Gianesello L, Trimarchi H, Migliorini A, Priante G, Radu CM, Naso E, Angelini A, Calò LA, Anglani F, Del Prete D. Ceol M, et al. J Nephrol. 2023 Dec;36(9):2499-2506. doi: 10.1007/s40620-023-01725-6. Epub 2023 Aug 18. J Nephrol. 2023. PMID: 37594671 Free PMC article.

2

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Priante G, Ceol M, Gianesello L, Bizzotto D, Braghetta P, Calò LA, Del Prete D, Anglani F. Priante G, et al. Int J Mol Sci. 2023 Jan 9;24(2):1313. doi: 10.3390/ijms24021313. Int J Mol Sci. 2023. PMID: 36674829 Free PMC article.

3

A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations.

Mollataheri A, Mojbafan M, Hosseini R, Houman N, Mousavi M, Otoukesh H. Mollataheri A, et al. Nephron. 2023;147(8):470-477. doi: 10.1159/000528344. Epub 2023 Jan 16. Nephron. 2023. PMID: 36646056

4

Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.

Deng H, Zhang Y, Xiao H, Yao Y, Zhang H, Liu X, Su B, Guan N, Zhong X, Wang S, Ding J, Wang F. Deng H, et al. Mol Genet Genomic Med. 2020 Aug;8(8):e1306. doi: 10.1002/mgg3.1306. Epub 2020 Jun 3. Mol Genet Genomic Med. 2020. PMID: 32495484 Free PMC article.

5

Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.

Inoue T, Nagano C, Matsuo M, Yamamura T, Sakakibara N, Horinouchi T, Shibagaki Y, Ichikawa D, Aoto Y, Ishiko S, Ishimori S, Rossanti R, Iijima K, Nozu K. Inoue T, et al. Clin Exp Nephrol. 2020 Jul;24(7):606-612. doi: 10.1007/s10157-020-01876-x. Epub 2020 Mar 22. Clin Exp Nephrol. 2020. PMID: 32201916 Free PMC article.

6

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

Ceol M, Gianesello L, Tosetto E, Priante G, Del Prete D, Anglani F. Ceol M, et al. J Investig Med. 2020 Apr;68(4):864-869. doi: 10.1136/jim-2019-001205. Epub 2020 Feb 3. J Investig Med. 2020. PMID: 32019767 Free PMC article.

7

Cl^- and H⁺ coupling properties and subcellular localizations of wildtype and disease-associated variants of the voltage-gated Cl^-/H⁺ exchanger ClC-5.

Chang MH, Brown MR, Liu Y, Gainullin VG, Harris PC, Romero MF, Lieske JC. Chang MH, et al. J Biol Chem. 2020 Feb 7;295(6):1464-1473. doi: 10.1074/jbc.RA119.011366. Epub 2019 Dec 18. J Biol Chem. 2020. PMID: 31852738 Free PMC article.

8

Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.

Ye Q, Shen Q, Rao J, Zhang A, Zheng B, Liu X, Shen Y, Chen Z, Wu Y, Hou L, Jian S, Wei M, Ma M, Sun S, Li Q, Dang X, Wang Y, Xu H, Mao J; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of National Center for Children's Care. Ye Q, et al. Clin Genet. 2020 Mar;97(3):407-417. doi: 10.1111/cge.13663. Epub 2020 Jan 13. Clin Genet. 2020. PMID: 31674016

9

ClC-5 alleviates renal fibrosis in unilateral ureteral obstruction mice.

Yang SX, Zhang ZC, Bai HL. Yang SX, et al. Hum Cell. 2019 Jul;32(3):297-305. doi: 10.1007/s13577-019-00253-5. Epub 2019 May 3. Hum Cell. 2019. PMID: 31054069

10

Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts.

Beara-Lasic L, Cogal A, Mara K, Enders F, Mehta RA, Haskic Z, Furth SL, Trachtman H, Scheinman SJ, Milliner DS, Goldfarb DS, Harris PC, Lieske JC; investigators of the Rare Kidney Stone Consortium. Beara-Lasic L, et al. Pediatr Nephrol. 2020 Apr;35(4):633-640. doi: 10.1007/s00467-019-04210-0. Epub 2019 Mar 10. Pediatr Nephrol. 2020. PMID: 30852663 Free PMC article.

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